A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18175362



Internal ID20742402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:118677874..118678177hg38UCSC Ensembl
chr9:121440152..121440455hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6453038
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18175362
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.02035


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